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8-Methoxycarbonyloctanoyl2,3,4,6-tetra-O-acetyl-b-D-galactopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 104494-93-1 Structure
  • Basic information

    1. Product Name: 8-Methoxycarbonyloctanoyl2,3,4,6-tetra-O-acetyl-b-D-galactopyranoside
    2. Synonyms: Nonanoic acid, 9-[(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)oxy]-, methyl ester
    3. CAS NO:104494-93-1
    4. Molecular Formula: C24H38 O12
    5. Molecular Weight: 518.55
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 104494-93-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 549.2±50.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.19±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 8-Methoxycarbonyloctanoyl2,3,4,6-tetra-O-acetyl-b-D-galactopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: 8-Methoxycarbonyloctanoyl2,3,4,6-tetra-O-acetyl-b-D-galactopyranoside(104494-93-1)
    11. EPA Substance Registry System: 8-Methoxycarbonyloctanoyl2,3,4,6-tetra-O-acetyl-b-D-galactopyranoside(104494-93-1)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 104494-93-1(Hazardous Substances Data)

104494-93-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104494-93-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,4,9 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 104494-93:
(8*1)+(7*0)+(6*4)+(5*4)+(4*9)+(3*4)+(2*9)+(1*3)=121
121 % 10 = 1
So 104494-93-1 is a valid CAS Registry Number.

104494-93-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-Methoxycarbonyloctanoyl2,3,4,6-tetra-O-acetyl-b-D-galactopyranoside

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:104494-93-1 SDS

104494-93-1Relevant articles and documents

Polymer-resin hybrid capture-release strategy for rapid oligosaccharide construction

Hanashima, Shinya,Manabe, Shino,Ito, Yukishige

, p. 979 - 982 (2007/10/03)

The polymer-resin hybrid type capture-release purification strategy for oligosaccharide synthesis was renewed as more rapid and straightforward manner. The substrate for N-acetylglucosaminyltransferase V trisaccharide was synthesized rapidly on PEG (poly (ethylene glycol) methyl ether) and purified by use of the strategy.

NEPHROTROPIC DRUGS

-

, (2008/06/13)

Disclosed are a drug having renal selectivity and a drug carrier for specifically transporting a drug supported thereon to a kidney. A segment structure specifically recognizable in the kidney is utilized. More specifically, since a segment structure repr

Synthesis and antidiuretic activities of novel glycoconjugates of arginine-vasopressin

Susaki, Hiroshi,Suzuki, Kokichi,Ikeda, Masahiro,Yamada, Harutami,Watanabe, Hiroshi K.

, p. 1530 - 1537 (2007/10/03)

Arginine-vasopressin (AVP) was acylated with various acyl azides (2a-j) in pH 9.1 buffer to give AVP derivatives (11a-j) modified at the tyrosine side chain with a carbohydrate via a spacer arm. Glycoconjugates of AVP modified at the N-terminal amide (12a

Syntheses of spacer-armed carbohydrate model compounds

Kerekgyarto, Janos,Nagy, Zoltan,Szurmai, Zoltan

, p. 107 - 115 (2007/10/03)

Commercially available chemicals, such as diethylene glycol, 1,9-nonanediol, 9-decen-1-ol, 1,2,6-hexanetriol, and p-nitrophenol were used to prepare spacer-armed carbohydrate derivatives. Glycosides of D-glucose, N-acetyl-D-glucosamine and 3-O-methyl-D-glucose have been synthesized, carrying reactive groups at the end of the spacer-arms. These glycosides are capable of forming neoglycoproteins. When bromo sugars were reacted with highly apolar aglycones in the presence of mercuric cyanide or mercuric bromide, a considerable amount of '2-OH-compounds' (such as 9-hydroxynonyl 3,4,6-tri-O-acetyl-β-D-glucopyranoside) were formed. Some spacer-armed derivatives (such as 9,10-epoxydecyl β-D-glucopyranoside) are theoretically a mixture of diastereomers, but this fact does not mirror in the 1H and 13C NMR spectra.

Combined glycomimetic and multivalent strategies for the design of potent selectin antagonists

Roy, Rene,Park, William K. C.,Srivastava, Om P.,Foxall, Carrol

, p. 1399 - 1402 (2007/10/03)

Stepwise large scale synthesis of 3'-sulfo-Lewis(X)-Glc mimetic of the lead anti-inflammatory agent sialyl Lewis(X) in a form suitable for copolymerization with acrylamide has been achieved. The resulting water- soluble copolyacrylamide showed inhibition of binding of both L- and E- selectins in the μMolar range.

SYNTHESIS OF IMMUNOSUPPRESIVE NEOGLYCOPROTEINS: BOVINE SERUM ALBUMIN COUPLED WITH 8-(HYDRAZINOCARBONYL)OCTYL 4- OR 6-O-&α-D-MANNOPYRANOSYL-&α-D-MANNOPYRANOSIDE

Wada, Kaoru,Chiba, Taku,Takei, Yutaka,Ishihara, Hideko,Hayashi, Hidetoshi,Onozaki, Kikuo

, p. 941 - 966 (2007/10/02)

Recombinant cytokines generated by bacteria, especially E.coli, are nonglycosylated.To investigate the effects of carbohydrates on their activities, we attempted to develop new cytokines by introduction of carbohydrates.As a model we synthesized neoglycop

Synthesis of phosphorylated trimannosides corresponding to end groups of the high-mannose chains of lysosomal enzymes.

Srivastava,Hindsgaul

, p. 195 - 210 (2007/10/02)

Glycosylation of suitably protected 8-methoxycarbonyloctyl alpha-D-manno-pyranosides with 2-O-acetyl-3,4,6-tri-O-benzyl-alpha-D-mannopyranosyl chloride provided alpha-D-Manp-(1----2)-alpha-D-Man, alpha-D-Manp-(1----3)-alpha-D-Man and alpha-D-Manp-(1----6)

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